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  • 3 days ago

    Constant Left Arm Pain - M.S. starting?

    About 4 months ago I started getting pains in my left arm. Original starting spot was Elbow area only. Then it expanding to about 3" below the Elbow but, not always both directions sometimes just one. Now periodically pain will go to ends of my fingers and/or top of my shoulder. The pain area changes as well as the pain severity frequently but the area that is constant, literally daily, is upper/outer elbow down about 3" to upper/outer forearm. Since it was changing frequently I kept telling....
  • 2 months ago

    Can give me some answer plz

    Allways tremours in my body,specially in my both hands.what might be the reason for that?
  • 2 months ago

    Misdiagnosed

    I was diagnosed with primary progressive multiple sclerosis, PPMS. Every symptom I’ve had is from my waist down, loss of mobility, urinary problem, GI problems and numbness with tingling sensations. The problem is I have no lesions. None on my brain and none in my CNS. I feel it could be something else. After reading the article on webmd I’m really convinced I’m one of those people the doctor who wrote the article is talking about. I would love to speak with her. Has anyone ever heard of this?
  • 4 months ago

    Diagnosis

    Hi there I have been having symptons for a couple of years now and the doctors can't seem to figure out exactly what I have. It first started in 2016 when I got a headache that felt like it was cracking my head open, just after the headache started I battled to look at any lights. This got increasingly worse and I started getting a fever. I was exhausted and could not stay awake. About 3 hours later I went to the doctor. They admitted me into hospital straight away suspecting meningitis. I was....
  • 6 months ago

    My TM is becoming MS.

    It seems the TM I have had since 2010 is morphing into MS. Apparently this is not uncommon. My hands are becoming shake, coordination is worse, my voice is beginning to quaver and I am even forgetting how to spell. Thoughts? Thanks
  • 7 months ago

    Maybe ms?

    I have tingling in my hands and feet, memory loss, shaky hands, fatigue and vertigo. These symptoms have all started in the last six months. I'm only 26, and have no ms history in my family that I'm aware of but all symptoms point to ms to me? Anyone else have these symptoms and were diagnosed with ms? What treatment do you receive? Or if not, what were you told was wrong of not ms? Thanks on advance!
  • 8 months ago

    Right eye very sensitive to light

    I am an MS patient and been dealing with different maladies. I am taking Gilenya for the MS. Just recently my right eye only has become very red, very painful, and very sensitive to light. September of 2018 I had another MRI with contrast. Could that be causing this latest issue? This has been going on since the last MRI. I am desperate for relief.
  • 10 months ago

    Numbness, No reflex +

    Hey everyone, this is my first time posting here, or even online at all really... But I will appologise for how long this might be before hand. I am a 23yo, female. Had a Microdiscectomy and Laminectomy when I was 18 and recovered with no deficits whatsoever. Around April last year (2018) so started to get a few symptoms of sciatica and some numbness of the outside of my left foot. I saw my doctor and had a scan. It's showed a small protrusion, and bone spurs. I was referred back to my neurosurgeon....
  • 11 months ago

    Resurgence of Symptoms

    About 6 years ago (I am 29 now) I went to the doctor with numbness and tingling in my left arm and leg as well as back pain. I was referred to a neurologist and after a battery of tests, I was sent for an MRI. The neuro said there were lesions present but not enough to diagnose. He said that it was more than likely stress. At the time that was ok with me because I was in the process of leaving a highly stressful job. Fast forward to today I have had symptoms on and off since the initial MRI but now....
  • 11 months ago

    Numbness, muscle twitching, and no diagnosis? Read this.

    I felt compelled to write this a year and a half after first experiencing neurological issues because #1, it seems that a lot of folks who have similar undiagnosed conditions simply "disappear" online (hopefully that means they've gotten better), and #2, I am still alive after a year and a half, so my goal is to give hope to anyone who is experiencing similar symptoms and have not had any luck with a diagnosis. First things first. If you have not seen any neurologists, stop reading....